CAS 6627-55-0

2-Bromo-4-methylphenol

Description:

2-Bromo-4-methylphenol, with the CAS number 6627-55-0, is an organic compound that belongs to the class of phenols. It features a bromine atom and a methyl group attached to a phenolic ring, specifically at the 2 and 4 positions, respectively. This compound is typically a white to light yellow solid and is known for its antimicrobial properties, making it useful in various applications, including as a preservative in cosmetics and personal care products. It has a moderate solubility in water and is more soluble in organic solvents. The presence of the bromine atom enhances its reactivity, allowing it to participate in various chemical reactions, such as nucleophilic substitutions. Additionally, 2-Bromo-4-methylphenol can exhibit both acidic and basic properties due to the hydroxyl group, which can donate a proton. Safety precautions should be taken when handling this compound, as it may pose health risks if ingested or inhaled, and appropriate protective equipment should be used.

Formula: C₇H₇BrO

InChI: InChI=1S/C7H7BrO/c1-5-2-3-7(9)6(8)4-5/h2-4,9H,1H3

InChI key: InChIKey=MTIDYGLTAOZOGU-UHFFFAOYSA-N

SMILES: BrC1=C(O)C=CC(C)=C1

Synonyms:

• 2-Bromo-4-cresol
• 2-Bromo-p-cresol
• 2-Bromo-p-cresol (OH=1)
• 3-Bromo-4-Hydroxytoluene
• NSC 60115
• Phenol, 2-bromo-4-methyl-
• p-Cresol, 2-bromo-
• 2-Bromo-4-methylphenol

2-Bromo-p-cresol

CAS: 6627-55-0

Formula: C₇H₇BrO

Purity: >98.0%(GC)

Color and Shape: White or Colorless to Light yellow powder to lump to clear liquid

Molecular weight: 187.04

Ref: 3B-B0808

2-Bromo-4-methylphenol, 97%

CAS: 6627-55-0

It is applied as a compound responsible for iodine off-flavor in wines. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU r

Formula: C₇H₇BrO

Purity: 97%

Color and Shape: Liquid, Clear colorless to yellow

Molecular weight: 187.04

Ref: 02-B21701

2-Bromo-4-methylphenol

CAS: 6627-55-0

2-Bromo-4-methylphenol

Formula: C₇H₇BrO

Purity: 97%

Color and Shape: Colourless Liquid

Molecular weight: 187.03388

Ref: 54-OR2424

2-Bromo-4-methylphenol

CAS: 6627-55-0

Formula: C₇H₇BrO

Purity: 98%

Color and Shape: Liquid

Molecular weight: 187.0339

Ref: IN-DA003GON

2-Bromo-4-methylphenol

Controlled Product

CAS: 6627-55-0

Applications 2-Bromo-4-methylphenol is a useful synthetic intermediate. It was used in the synthesis of furan-2-ylmethylene thiazolidinediones as potent, and selective inhibitors of phosphoinositide 3-kinase γ. It was also a reactant used to prepare phosphoramidate and phosphorothioamidate analogs of amiprophos Me as potential antimalarial agents.
References Pomel, V., et al.: J. Med. Chem., 49, 3857 (2006); Mara, C., et al.: Bioorg. Med. Chem. Lett., 21, 6180 (2011)

Formula: C₇H₇BrO

Color and Shape: Neat

Molecular weight: 187.03

Ref: TR-B686105

2-Bromo-4-methylphenol

CAS: 6627-55-0

2-Bromo-4-methylphenol

Formula: C₇H₇BrO

Purity: 95%

Molecular weight: 187.03

Ref: IN-DG34550

2-Bromo-4-methylphenol

CAS: 6627-55-0

Formula: C₇H₇BrO

Purity: 95%

Color and Shape: Liquid

Molecular weight: 187.036

Ref: 10-F092949

2-Bromo-4-methylphenol

CAS: 6627-55-0

2-Bromo-4-methylphenol is an organic compound that has interactive effects with hydrochloric acid, molybdenum, and trifluoromethanesulfonic acid. It is soluble in water vapor, but insoluble in polyvinyl. 2-Bromo-4-methylphenol reacts with sodium hydroxide solution to form a hydroxide solution and sodium carbonate. The reaction product of 2-bromo-4-methylphenol with triterpenoid saponin produces fatty acids. This reaction occurs because the hydroxide ion from the sodium hydroxide solution attacks the ester group of the saponin, forming an alcohol group on one end and a carboxylic acid group on the other end. The benzyl groups are removed by hydrogenation to produce phenol.

Formula: C₇H₇BrO

Purity: Min. 95%

Molecular weight: 187.03 g/mol

Ref: 3D-FB33955